Label: BAN ROLL-ON ANTIPERSPIRANT DEODORANT REGULAR- aluminum chlorohydrate liquid
- NDC Code(s): 10596-336-14, 10596-336-15, 10596-336-35, 10596-336-70
- Packager: Kao USA Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated August 18, 2023
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
- STOP USE
- ASK DOCTOR
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- STORAGE AND HANDLING
-
INACTIVE INGREDIENT
Inactive ingredients
water, PPG-11 stearyl ether, steareth-2, steareth-20, fragrance, disodium EDTA, helianthus annuus (sunflower) seed oil, phellodendron amurense bark extract, hordeum distichon (barley) extract, santalum album (sandalwood) extract, amyl cinnamal, benzyl alcohol, benzyl benzoate, cinnamyl alcohol, citronellol, eugenol, geraniol, hexyl cinnamal, linalool
- SPL UNCLASSIFIED SECTION
- 44 mL PACKAGE
- 103 mL PACKAGE
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
BAN ROLL-ON ANTIPERSPIRANT DEODORANT REGULAR
aluminum chlorohydrate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10596-336 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE 20 g in 103 mL Inactive Ingredients Ingredient Name Strength PPG-11 STEARYL ETHER (UNII: S4G2J0Y0LG) WATER (UNII: 059QF0KO0R) STEARETH-2 (UNII: V56DFE46J5) STEARETH-20 (UNII: L0Q8IK9E08) SANDALWOOD (UNII: 3641YW25N2) PHELLODENDRON AMURENSE BARK (UNII: PBG27B754G) BARLEY (UNII: 5PWM7YLI7R) EDETATE DISODIUM (UNII: 7FLD91C86K) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) SUNFLOWER OIL (UNII: 3W1JG795YI) .ALPHA.-AMYLCINNAMALDEHYDE (UNII: WC51CA3418) BENZYL ALCOHOL (UNII: LKG8494WBH) CINNAMYL ALCOHOL (UNII: SS8YOP444F) .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K) GERANIOL (UNII: L837108USY) .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I) LINALOOL, (+/-)- (UNII: D81QY6I88E) BENZYL BENZOATE (UNII: N863NB338G) EUGENOL (UNII: 3T8H1794QW) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10596-336-35 103 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 01/01/2012 2 NDC:10596-336-70 2 in 1 PACKAGE 09/12/2016 2 103 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 3 NDC:10596-336-15 44 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 11/04/2016 4 NDC:10596-336-14 4 in 1 PACKAGE 12/12/2019 4 103 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part350 01/01/2012 Labeler - Kao USA Inc. (004251617)
